ProfileGDS1065 / 210663_s_at
TitleMitochondrial encephalomyopathies associated with mitochondrial DNA mutations
OrganismHomo sapiens


wild type A3243G large deletion normal MELAS PEO GSM24652 GSM24653 GSM24654 GSM24655 GSM24656 GSM24657 GSM24658 GSM24659 GSM24660 GSM24661 GSM24662 GSM24663 GSM24664 GSM24665 GSM24666 17% 22% 13% 15% 14% 13% 15% 19% 17% 14% 12% 21% 13% 12% 13% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.117
GSM24653Normal subject 29.722
GSM24654Normal subject 35.813
GSM24655A3243G-MELAS subject 15.215
GSM24656A3243G-MELAS subject 26.614
GSM24657A3243G-MELAS subject 36.813
GSM24658A3243G-MELAS subject 4515
GSM24659A3243G-PEO subject 18.219
GSM24660A3243G-PEO subject 27.317
GSM24661A3243G-PEO subject 34.314
GSM24662A3243G-PEO subject 44.312
GSM24663mtDNA "Common"-deletion subject 19.421
GSM24664mtDNA "Common"-deletion subject 29.813
GSM24665mtDNA "Common"-deletion subject 36.812
GSM24666mtDNA "Common"-deletion subject 46.813